Accenture Hiring LifeScience Regulatory Svs Analyst

LifeScience Regulatory Svs Analyst Opportunity

Are you a qualified M.Pharm professional with experience in regulatory affairs? Accenture, a global leader in professional services, is seeking skilled candidates to join its Life Sciences Regulatory Services team in Bengaluru. If you have 3–5 years of experience, this is your chance to work with a company that thrives on innovation and human ingenuity.

About Accenture

Accenture is at the forefront of digital transformation, offering unmatched expertise in cloud, security, and advanced technologies. With operations in over 120 countries, the company is committed to improving outcomes across industries, including life sciences R&D. Accenture’s mission is to empower clients to achieve their goals while fostering a culture of excellence, innovation, and inclusivity.

Role Details: LifeScience Regulatory Svs Analyst

Job Title: LifeScience Regulatory Svs Analyst

• Location: Bengaluru, Karnataka
• Department: Life Sciences Regulatory Services
• Qualification: Master of Pharmacy (M.Pharm)
• Experience Required: 3 to 5 years in regulatory affairs
• Language Proficiency: Expert in English

Key Responsibilities

Regulatory Compliance and Documentation:

• Build regulatory dossiers in accordance with ICH guidelines and health authority requirements.
• Perform Quality Control (Document QC) checks on submission components.
• Author CMC documents and regulatory submissions for health authorities.

Data Analysis and Evaluation:

• Collect, collate, and evaluate scientific data as part of research and development.
• Provide guidance on legal and scientific requirements to ensure compliance with current regulations.

Collaboration and Problem-Solving:

• Work as an individual contributor within a team.
• Collaborate with peers and supervisors to address low-complexity problems.
• Contribute to improving processes and delivering high-quality outputs.

What Accenture Looks For

Key Skills:

• Expertise in Life Sciences Regulatory Services.
• Adaptability, attention to detail, and problem-solving abilities.
• Agility for quick learning and performing under pressure.

Ideal Candidate Profile:

• A detail-oriented professional passionate about regulatory compliance and improving patient outcomes.
• Someone who thrives in a collaborative environment and is eager to contribute to cutting-edge projects.

How to Apply

Interested in joining Accenture’s innovative team? Apply online today by visiting the link below:
👉 Apply Now at Accenture Careers

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Jobs